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New · posted Nov 1

ICON · Pharmaceuticals

Clinical Trial Manager II

  • Blue Bell, PA
  • On-site
  • Full-time
  • Manager
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EmploymentFull-time
DeadlineOpen until filled

The role

Clinical Trial Manager

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Clinical Trial Manager II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What you need

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • Bachelor's degree in a relevant field, with a minimum of 5 years of experience in clinical trial management.
  • Proven expertise in designing and executing clinical trials, with a strong understanding of regulatory requirements.
  • Exceptional analytical and problem-solving skills, with the ability to interpret complex medical data.
  • Effective communication and interpersonal skills, with the ability to collaborate across diverse teams.
  • Detail-oriented and organized, with a track record of successfully managing multiple tasks and priorities simultaneously.
  • Willingness to travel as required (approximately 10%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

What you'll do

You will oversee clinical trial management workstreams, ensuring deliverables meet quality and timeline expectations.

Key responsibilities include:

  • Collaborate with cross-functional teams to design and implement effective clinical trial enrollment Collaborating with cross-functional teams to develop and implement comprehensive clinical trial protocols.
  • Overseeing and managing the day-to-day operations of clinical trials, ensuring compliance with regulatory standards.
  • Analyzing and interpreting clinical trial data, identifying trends, and providing insights to optimize study outcomes.
  • Proactively addressing challenges and implementing effective solutions to ensure the successful execution of clinical trials.
  • Communicating effectively with internal and external stakeholders to foster strong partnerships and facilitate smooth trial processes.

Pay and benefits

ICON didn't publish pay for this role

See what similar roles pay on Regulatory Jobs, or try the salary calculator.

Rewards & Benefits

  • Competitive base salary and performance related incentives

  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable

  • Retirement and pension plans

  • Life assurance and disability coverage

  • Employee assistance programmes and wellbeing resources

  • Learning and development opportunities through structured training and career pathways

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Where you'll work

Blue Bell, PAOn-siteOpen in Maps (opens in a new tab)

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Equal opportunity, accessibility and legal noticesICON's statements, word for word

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Job intelligence

The context around this role

Live data · November 1, 2026

Salary intelligence

How the pay compares

Manager roles in the US44 roles publishing pay

Middle half $150,125 to $175,000, median $163,000
Annual base pay
Annual base payLowMedianHigh
All US$150,125$163,000$175,000

Comparisons: the base pay employers published on open Clinical Trial Management roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Trial Management

The general path across 69 open Clinical Trial Management roles on Regulatory Jobs, with the titles they carry most. Not ICON's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Clinical Trial Assistant · Clinical Study Specialist

    $87K median7 open
  2. One step back

    Senior & Principal

    Often: Regional Clinical Trial Management Senior Associate · Clinical Research Leader

    $131K median6 open
  3. This role

    Manager

    Often: Senior Clinical Trial Manager · Clinical Trial Manager

    $163K median55 open
  4. Next step

    Director

    Often: Associate Director, Clinical Development Trial Lead

Skills DNA

What this role leans on

How many of the posting's 18 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 1 lineLab testing and methods: 2 linesDocumentation and SOPs: 1 lineClinical trial conduct: 10 linesCollaboration and leadership: 5 linesGMPLab testingDocumentationClinical trialsTeamwork
  • Clinical trial conduct10
  • Collaboration and leadership5
  • Lab testing and methods2
  • GMP and compliance1
  • Documentation and SOPs1

Company hiring pulse

ICON on Regulatory Jobs

106
Open roles
56
Distinct roles
30
Locations

By discipline

  • Clinical96 91%
  • Quality7 7%
  • Regulatory3 3%

By level

  • Senior & Principal45 42%
  • Associate & Specialist43 41%
  • Manager15 14%
See all 106 ICON roles

More roles at ICON

All 106 ICON roles

Similar Clinical Trial Management roles elsewhere

Clinical Trial Manager II at ICON

Open until filled.

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